Johnson & Johnson jobs in Greenville, NC - 51 jobs

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at ******************* **Job Function:** Quality **Job Sub** **Function:** Quality Control **Job Category:** Professional **All Job Posting Locations:** Wilson, North Carolina, United States of America **:** Job Description Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow. Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way. Learn more at *******************/innovative-medicine We are seeking an experienced **Bioassay Specialist** with strong expertise in **cell-based and ligand-binding assays** , specifically **Antibody-Dependent Cellular Cytotoxicity (ADCC)** , **Complement-Dependent Cytotoxicity (CDC)** , and **Enzyme-Linked Immunosorbent Assay (ELISA)** , to join our Quality Control (QC) team at a newly established large molecule manufacturing site in Wilson, NC. As one of the first fifteen employees in the QC department, you will play a critical role in building laboratory capabilities, authoring procedures, and transferring complex bioassay methods in a GMP-regulated environment. J&J is expanding our manufacturing capacity with $2 billion investment to support strong portfolio growth and continue delivering breakthrough innovation and transformational medicines for patients. The new facility will expand production of innovative biologic medicines in areas including oncology, immunology, and neuroscience. J&J's significant supply chain investment ensures a resilient and reliable future supply of medicines to meet accelerating demand for our current portfolio of medicines and our future innovations. **Key Responsibilities** + **Establish QC Bioassay Capabilities:** Support the build-out of QC laboratory infrastructure and workflows for potency and immunoassays. + **Method Transfer & Validation:** Lead comparative testing and transfer of ADCC, CDC, and ELISA methods for biologics, ensuring compliance with global regulatory standards (FDA, EMA, ICH). + **Procedure Development:** Author, review, and approve SOPs, work instructions, and technical documentation for bioassay testing. + **Technical Expertise:** Serve as the subject matter expert for bioassay techniques; train and mentor incoming QC personnel on assay execution and data integrity principles. + **Cross-Functional Collaboration:** Partner with MSAT, QA, and Operations to ensure seamless method implementation and resolve technical challenges during scale-up and commercialization. + **Compliance & Quality:** Maintain adherence to GMP, compendial requirements, and site-specific quality standards. Support regulatory inspections and contribute to observation responses. + **Continuous Improvement:** Identify and implement process improvements to enhance efficiency and robustness of bioassay testing. **Qualifications** + Bachelor's degree in Biology, Biochemistry, Immunology, or related field; advanced degree preferred. + Minimum 6 years of experience in QC or analytical development within biologics or pharmaceutical manufacturing. + Strong expertise in ADCC, CDC, and ELISA assays, with proven experience in method validation, transfer, and regulatory compliance in a GMP environment. + Knowledge of compendial standards and global regulatory guidelines. + Excellent communication skills and ability to thrive in a dynamic, start-up environment. **Key Competencies** + Entrepreneurial mindset with a passion for building new capabilities. + Detail-oriented and highly organized, with strong problem-solving skills. + Ability to work independently and collaboratively across functions. Johnson & Johnson is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, protected veteran status or other characteristics protected by federal, state or local law. We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act. Johnson and Johnson is committed to providing an interview process that is inclusive of our applicants' needs. If you are an individual with a disability and would like to request an accommodation, please email the Employee Health Support Center (********************************) or contact AskGS to be directed to your accommodation resource. **Required Skills:** **Preferred Skills:**

Bausch + Lomb (NYSE/TSX: BLCO) is a leading global eye health company dedicated to protecting and enhancing the gift of sight for millions of people around the world-from the moment of birth through every phase of life. Our mission is simple, yet powerful: helping you see better, to live better. Our comprehensive portfolio of over 400 products is fully integrated and built to serve our customers across the full spectrum of their eye health needs throughout their lives. Our iconic brand is built on the deep trust and loyalty of our customers established over our 170-year history. We have a significant global research, development, manufacturing and commercial footprint of approximately 13,000 employees and a presence in approximately 100 countries, extending our reach to billions of potential customers across the globe. We have long been associated with many of the most significant advances in eye health, and we believe we are well positioned to continue leading the advancement of eye health in the future. Objectives | Purpose: The Material Handler is responsible for handling material flow by receiving, retrieving, and issuing components in support of production. Key Activities/Responsibilities: Perform warehousing tasks, such as: loading/unloading trucks, receiving materials, operating the Palletizer, pulling components against the shop order pick ticket to support the Packaging Lines, and any other assigned duties. Operate Hi-Racker (Turret) and Sit-Down Forklift powered industrial equipment (PIT) to support the Packaging/Warehouse functions. Utilize ERP Lx and RF units to accurately perform material transactions and issue components to shop orders. Prepare outbound shipments for pickup. Support continuous improvement initiatives. The Material Handler's responsibility is to ensure safe/efficient operation of the PIT equipment and ERP Lx in a way that meets quality requirements and conforms to all regulatory requirements. Qualifications | Training: Education: High School Diploma or equivalent preferred. Experience: * Certified Forklift Driver with working operational knowledge of warehouse equipment. Example: Pallet Jacks, Palletizer, Sit-Down Forklift, and Hi-Racker (Turret) experience preferred. * 1-year experience operating Powered Industrial Equipment required. * Working in a Manufacturing or Distribution Center environment preferred. * Warehouse Management Systems experience preferred (ERP Lx). Skills: Strong reading and math comprehension, excellent communication skills (written & verbal), good attention to detail, demonstrated problem-solving ability, works well in team environment. Computer skills to include MS Outlook & Excel, ability to navigate web-based computer applications. Shift | Hours: WE Shift | Sat/Sun 7am-7p + Wed/Thurs 3:30p-12a Salary: $18.50 per hour plus $2.25 weekend shift differential. This position may be available in the following location: Greenville, SC All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status. Job Applicants should be aware of job offer scams perpetrated through the use of the Internet and social media platforms To learn more please read Bausch + Lomb's Job Offer Fraud Statement. Our Benefit Programs: Employee Benefits: Bausch + Lomb Applicants must be authorized to work for ANY employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time.

Bausch + Lomb (NYSE/TSX: BLCO) is a leading global eye health company dedicated to protecting and enhancing the gift of sight for millions of people around the world-from the moment of birth through every phase of life. Our mission is simple, yet powerful: helping you see better, to live better. Our comprehensive portfolio of over 400 products is fully integrated and built to serve our customers across the full spectrum of their eye health needs throughout their lives. Our iconic brand is built on the deep trust and loyalty of our customers established over our 170-year history. We have a significant global research, development, manufacturing and commercial footprint of approximately 13,000 employees and a presence in approximately 100 countries, extending our reach to billions of potential customers across the globe. We have long been associated with many of the most significant advances in eye health, and we believe we are well positioned to continue leading the advancement of eye health in the future. Objectives/Purpose of Job: Effectively and efficiently set-up, troubleshoot and operate packaging lines and equipment in order to manufacture quality products per Standard Operating Procedures (SOP) and Good Manufacturing Practices (GMP). Key Activities/Responsibilities: Adhere to Standard Operating Procedures and GMP's. Set-up and Operate Packaging equipment (Labeler, Cartoner, Bundler, Case Packer, Lens Caser, Print & Apply Labeler, Automated bulk machines and Filtec). Keep steady supply of components in each machine. Perform line clearances and sublot changeover. Accurately perform and document Quality Inspections, In-process Cosmetic Inspections, Tank Changeovers, and Batch Record related information (verification of components and critical copy information). Data Entry which includes recording downtime and standard yield. Housekeeping. Scope of Position: Effectively and efficiently set-up, troubleshoot and operate packaging lines and equipment in order to manufacture quality products per Standard Operating Procedures (SOP) and Good Manufacturing Practices (GMP). Qualifications | Training: Education: High School Diploma or equivalent education preferred. Experience: Minimum one (1) year manufacturing experience, preferably in a packaging operation, two (2) or four (4) year degree, or manufacturing certification. Preferred Skills: * Strong reading and math comprehension * Good communication skills (written & verbal) * Ability to be an effective member of a team * Ability to work with minimal supervision * Ability to prioritize work and make informed decisions * Basic computer skills (i.e. MS Outlook, Excel, web-based applications) * PLC machine/equipment experience preferred Shift Weekend: Saturday, Sunday 7:00am - 7:00pm plus 2 8 hour shifts during the week. Pay starts at $18.00 per hour plus $2.25 per hour shift differential. This position may be available in the following location: Greenville, SC All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status. Job Applicants should be aware of job offer scams perpetrated through the use of the Internet and social media platforms. To learn more please read Bausch + Lomb's Job Offer Fraud Statement. Our Benefit Programs: Employee Benefits: Bausch + Lomb Applicants must be authorized to work for ANY employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time.

We are Reckitt Home to the world's best loved and trusted hygiene, health, and nutrition brands. Our purpose defines why we exist: to protect, heal and nurture in the relentless pursuit of a cleaner, healthier world. We are a global team united by this purpose. Join us in our fight to make access to the highest quality hygiene, wellness, and nourishment a right and not a privilege. Supply Our supply chain is the backbone of our business. It's how we get our trusted products to people all over the world, safely and efficiently. And it's our talented and passionate teams that make this happen. If you're looking for a career in supply chain, there's no better place to be than Reckitt. We offer a variety of exciting opportunities in all areas of the supply chain, from planning and procurement to manufacturing and logistics. You could join our Global Supply Planning team to develop and implement our global supply strategy, or work with our Procurement Centre of Excellence team to negotiate and manage our supplier relationships. Our Manufacturing Excellence team help us improve the efficiency, quality and safety of our manufacturing operations, and our Logistics Excellence team develop new and innovative ways to distribute our products to customers. About the role The Maintenance & Materials Planner for solid dose manufacturing is responsible for planning, scheduling, and coordinating maintenance activities by ensuring necessary parts, materials, and resources are available when needed. This role supports equipment reliability, safety compliance, and operational efficiency by developing detailed job plans, managing preventive maintenance schedules, and maintaining accurate records in the CMMS. The Planner collaborates closely with production, maintenance staff, and other departments to minimize downtime and optimize maintenance execution. Your responsibilities Resource and Workforce Support * Develop, prioritize, and schedule corrective, preventive, and predictive maintenance work orders for OSD production equipment (granulators, fluid bed dryers, tablet presses, coaters, blending equipment, utilities, and packaging lines). * Prepare detailed work orders and job plans including material lists, labor estimates, and safety requirements. * Assist in coordinating maintenance staff and contractors to align with production schedules. * Support backlog management and ensure planned jobs are properly resourced. Materials and Inventory Management * Ensure parts and materials are ordered, available, and "kitted" for planned jobs. * Manage spare parts inventory and research cost-effective, quality parts. * Evaluate repair vs. replacement options to optimize costs. Maintenance Planning and Scheduling * Develop preventive and corrective maintenance schedules to minimize downtime. * Coordinate with production supervisors and maintenance staff to align maintenance with operational needs. * Track and report on maintenance KPIs such as uptime, backlog, and work order completion rates. Communication & Coordination * Facilitate daily maintenance planning meetings with Operations and Maintenance * Communicate schedule updates, job delays, and resource gaps. * Provide clear instructions and support to maintenance technicians to ensure successful job execution. Data and System Management * Enter and update maintenance information in CMMS. * Maintain accurate equipment files, specifications, and job history. * Review and screen incoming work requests for clarity, priority, and required resources Process Improvement and Compliance * Optimize preventive maintenance (PM) frequencies, job plans, and procedures based on technician feedback, equipment performance, and reliability data. * Identify and eliminate potential delays in maintenance execution. * Ensure all maintenance work complies with OSHA and company safety standards. * Support continuous improvement initiatives to enhance efficiency and reliability. This role is not currently sponsoring visas or considering international movement at this time. The experience we're looking for * High school diploma or equivalent with several years of experience in a manufacturing or industrial environment * Strong understanding of mechanical and electrical systems, maintenance practices, precision tools, and OSHA safety regulations * Experience with maintenance planning, scheduling, backlog management, and preventive/predictive maintenance programs * Proficiency with CMMS platforms, including SAP, and general PC applications such as Word, Excel, and PowerPoint * Familiarity with spare parts management, cost‑optimization strategies, and performance‑metric tracking for continuous improvement * Strong planning and organizational abilities with the capacity to manage multiple projects * Effective written and verbal communication skills for cross‑department collaboration * Analytical problem‑solving skills to troubleshoot issues and develop solutions * Associate degree in a technical field or CMRP certification (preferred) The skills for success Supply Chain Management, Business Partnership, Collaboration and partnership building, Relationship Management, Business Acumen, Productivity management, Improve business processes, Advanced Analytics, Data Analytics, Supply Chain Planning, Logistics Management. What we offer With inclusion at the heart of everything we do, working alongside our four global Employee Resource Groups, we support our people at every step of their career journey, helping them to succeed in their own individual way. We invest in the wellbeing of our people through parental benefits, an Employee Assistance Program to promote mental health, and life insurance for all employees globally. We have a range of other benefits in line with the local market. Through our global share plans we offer the opportunity to save and share in Reckitt's potential future successes. For eligible roles, we also offer short-term incentives to recognise, appreciate and reward your work for delivering outstanding results. You will be rewarded in line with Reckitt's pay for performance philosophy. US salary ranges USD $69,000.00 - $103,000.00 Hiring Range up to 85K US pay transparency The base salary range for this role will vary based on experience in job and industry, training and education, skills relevant to the position, and other factors permitted by law. In addition to the base salary, the position is eligible for an annual discretionary bonus, which is subject to change each year. Reckitt offers eligible employees competitive benefits including medical, prescription, dental, vision, and life and disability insurance; paid time off for vacation, sick and Company recognized holidays; a 401(k) plan; 16-week paid parental leave or 26 weeks for the birthing parent; adoption and fertility support; tuition reimbursement; discounts; and much more. Our compensation and benefits packages aim to give our talent the reward, protection, and peace of mind they deserve. If reasonable accommodation is needed to complete your application, please contact *******************************. Reckitt is committed to the full inclusion of all qualified individuals. Equality We recognise that in real life, great people don't always 'tick all the boxes'. That's why we hire for potential as well as experience. Even if you don't meet every point on the job description, if this role and our company feels like a good fit for you, we still want to hear from you. All qualified applicants will receive consideration for employment without regard to age, disability or medical condition; colour, ethnicity, race, citizenship, and national origin; religion, faith; pregnancy, family status and caring responsibilities; sexual orientation; sex, gender identity, gender expression, and transgender identity; protected veteran status; size or any other basis protected by appropriate law. Nearest Major Market: Raleigh Nearest Secondary Market: Rocky Mount Job Segment: Counseling, Nutrition, Healthcare

Bausch + Lomb (NYSE/TSX: BLCO) is a leading global eye health company dedicated to protecting and enhancing the gift of sight for millions of people around the world-from the moment of birth through every phase of life. Our mission is simple, yet powerful: helping you see better, to live better. Our comprehensive portfolio of over 400 products is fully integrated and built to serve our customers across the full spectrum of their eye health needs throughout their lives. Our iconic brand is built on the deep trust and loyalty of our customers established over our 170-year history. We have a significant global research, development, manufacturing and commercial footprint of approximately 13,000 employees and a presence in approximately 100 countries, extending our reach to billions of potential customers across the globe. We have long been associated with many of the most significant advances in eye health, and we believe we are well positioned to continue leading the advancement of eye health in the future. The Sterilizer Operator will load/unload totes and place dosimeters on product. Transfer pre-sterilized product into the APA. Unload trucks of non-sterile components from vendors and prepare them for processing while ensuring separation of sterile and non-sterile components. Place and read dosimeters using a digital micrometer and spectrophotometer. Operate Irradiator Console to set timer settings and clear faults/settings. PC Data entry to include dosimetry information and basic inventory receipt transactions in ERP Lx. Analyze and correct irradiator faults by interpreting program logic controller display indicators and repositioning switches, totes and sensors on the source pass as well as the entry and exit conveyors. Operate industrial irradiator and will load and unload components to ensure proper sterilization during irradiation operations. Education: HS Diploma/GED preferred. Radiation Safety and Forklift Certification preferred. Aseptic environment experience a plus. Warehouse Management Systems experience preferred (ERP Lx). Experience: 2 years of manufacturing experience required or advanced education degree (2 or 4 year). Preferred Skills: Strong reading and math comprehension, excellent communication skills (written & verbal), good attention to detail, demonstrated problem-solving ability. Computer skills to include MS Outlook & Excel, ability to navigate web-based computer applications. Shift: Rotating 12-Hour Nights | 6:00p - 6:00a Starting Salary: $20.00 per hour plus $1.00 per hour shift differential This position may be available in the following location: Greenville, SC All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status. Job Applicants should be aware of job offer scams perpetrated through the use of the Internet and social media platforms. To learn more please read Bausch + Lomb's Job Offer Fraud Statement. Our Benefit Programs: Employee Benefits: Bausch + Lomb Applicants must be authorized to work for ANY employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time.

Bausch + Lomb (NYSE/TSX: BLCO) is a leading global eye health company dedicated to protecting and enhancing the gift of sight for millions of people around the world-from the moment of birth through every phase of life. Our mission is simple, yet powerful: helping you see better, to live better. Our comprehensive portfolio of over 400 products is fully integrated and built to serve our customers across the full spectrum of their eye health needs throughout their lives. Our iconic brand is built on the deep trust and loyalty of our customers established over our 170-year history. We have a significant global research, development, manufacturing and commercial footprint of approximately 13,000 employees and a presence in approximately 100 countries, extending our reach to billions of potential customers across the globe. We have long been associated with many of the most significant advances in eye health, and we believe we are well positioned to continue leading the advancement of eye health in the future. OVERVIEW: This position is responsible for executing the Greenville Sterile Filling Department's training schedule, deliver various training programs to a wide associate base which includes Sterile Filling Department employees, Maintenance Personnel and other Bausch & Lomb Associates that will be working in the APA. Maintaining and monitoring aseptic technique and compliance in the entire APA.Maintain associate training records within the current LMS system to ensure accurate reporting and metrics. Partner with the Training department to design and develop Filling department training courses. KEY ACTIVITIES/RESPONSIBILITIES Duties include, but are not limited to: Monitor Aseptic Processing and Technique compliance across all shifts including Sterile Prep Maintain APA Gowning Certification Develop and oversee the Sterile Filling Department's training planning and scheduling Perform "on the job" training Perform class room sessions including the APA Basic Gowning Course Administer all qualification events Perform requalification activities Will oversee all associated training administrative items Will ensure that the Filling Department complies to all associated training performance goals Will gather and report training metrics per the mandated schedule Will perform training gap analysis as required Will work with the Training department to revise/update the Sterile Filling Department's training material and curriculums as required Will perform training effectiveness verifications using the industry standard methodology HOURS: 2nd Shift | Monday - Friday | 3:30pm - 12:00midnight SCOPE OF POSITION: Lead on-the-job trainer for the APA KEY RELATIONSHIPS: Internal customers/partners: Trainer will work with multiple departments within the operations group. External customers: Regulatory Agencies and Notified Bodies. EDUCATION AND EXPERIENCE: Education: High School diploma or equivalent required: college level degree preferred. Specialized Training: Train the Trainer certification preferred, competency in Microsoft Outlook, Microsoft Excel, Microsoft Word preferred. This position may be available in the following location: Greenville, SC All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status. Job Applicants should be aware of job offer scams perpetrated through the use of the Internet and social media platforms. To learn more please read Bausch + Lomb's Job Offer Fraud Statement. Our Benefit Programs: Employee Benefits: Bausch + Lomb Applicants must be authorized to work for ANY employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time.

At Bayer we're visionaries, driven to solve the world's toughest challenges and striving for a world where 'Health for all Hunger for none' is no longer a dream, but a real possibility. We're doing it with energy, curiosity and sheer dedication, always learning from unique perspectives of those around us, expanding our thinking, growing our capabilities and redefining 'impossible'. There are so many reasons to join us. If you're hungry to build a varied and meaningful career in a community of brilliant and diverse minds to make a real difference, there's only one choice. Primary Care Sales Consultant - Greenville / Raleigh, NC Primary Care Sales Consultant - Greenville / Raleigh, NC PURPOSE Primary Care Sales Consultant (SC) is accountable for implementing the sales strategies for approved an approved Cardiorenal product. You will further drive launch activities for an anticipated launch for menopause. Responsibilities of the role include driving demand, clinical education and sales by developing, coordinating, and implementing a strategic business plan for Primary Care Physicians, primarily in the Community settings. The position reports to the CVR Area General Manager (AGM) and will be an integral part of the Area Customer Squad, collaborating closely with Marketing, Market Access, Patient Services, and other internal partners, as appropriate, to drive the US Pharma outcomes. The span of coverage will be within the Greenville / Raleigh, NC metro areas. Travel up to 50% within the territory. The position is residence based and candidate must be domiciled within the territory. YOUR TASKS AND RESPONSIBILITIES The primary responsibilities of this role, Primary Care Sales Consultant are to: * Build and develop professional relationships with (but not limited to) primary care, pharmacy staff, within assigned customers; * Drive appropriate utilization of approved CV and menopause products; the incumbent will work closely with the Customer Squad to generate pull-through within local payers, community HCPs; * Leverage expertise and knowledge of diabetes and menopause marketplace, applicable competitors, industry and cross-functional activities/plans to anticipate and effectively manage business opportunities and challenges; * Provide relevant, thoughtful input to other commercial colleagues (e.g. sales leadership, regional account managers) in regard to strategic and tactical planning for territory, area, and region; * Develop and implement effective customer specific business plans; communicates insights to internal stakeholders; * Prioritize time and effort to ensure optimal coverage of appropriate physician specialists based on opportunity and potential; * Understand fully the assigned customers' product and business needs and works to meet those needs while adhering to all of Bayer company ethics and compliance standards; * Anticipate potential barriers to achievement of goals and proposes responsible solutions for success; * Handle customer objections effectively and exceed customer expectations with the value they bring to physicians. Occasionally will be called on to share your exemplary skills with others in the region in a training capacity; * Leverage and embrace emerging technologies to enhance performance, while continuously striving to improve your proficiency; * Understand and comply with pharmaceutical industry guidelines and regulations and apply high ethical standard in day-to-day work. WHO YOU ARE Bayer seeks an incumbent who possesses the following: REQUIRED QUALIFICATIONS * Bachelor's degree or 10 years of relevant sales experience in competitive landscapes in lieu of a Bachelor's degree; * Proven track record of consistent high performance in a sales role or other relevant experience; * Proven track record in developing long-standing relationships with customers; * Outstanding written and oral communication skills; * Demonstrated leadership and foster an environment that promotes ethical behavior and compliance with company policies and applicable laws; * Ability to comply with any customer credentialing and safety requirements (e.g., up-to-date vaccinations, trainings); * Valid driver's license and clean driving record required. PREFERRED QUALIFICATIONS * An advanced degree is a plus; * 5 years of successful pharmaceutical/biotech/medical sales experience in competitive landscapes; * In depth knowledge in the cardiovascular and/or diabetes and/or menopause disease states; * Product launch experience; * Strong analytical and computer capabilities; * Virtual Sales Experience; * Strong local relationships with HCPs and understanding of local market. Employees can expect to be paid a salary between $120,960.00 to $181,440.00. Additional compensation may include a bonus or commission (if relevant). Additional benefits include health care, vision, dental, retirement, PTO, sick leave, etc. This salary range is merely an estimate and may vary based on an applicant's location, market data/ranges, an applicant's skills and prior relevant experience, certain degrees and certifications, and other relevant factors. This posting will be available for application until at least 1/23/26. #LI-US #LI-AMS YOUR APPLICATION Bayer offers a wide variety of competitive compensation and benefits programs. If you meet the requirements of this unique opportunity, and want to impact our mission Science for a better life, we encourage you to apply now. Be part of something bigger. Be you. Be Bayer. To all recruitment agencies: Bayer does not accept unsolicited third party resumes. Bayer is an Equal Opportunity Employer/Disabled/Veterans Bayer is committed to providing access and reasonable accommodations in its application process for individuals with disabilities and encourages applicants with disabilities to request any needed accommodation(s) using the contact information below. Bayer is an E-Verify Employer. Location:United States : North Carolina : Greenville || United States : North Carolina : Raleigh Division:Pharmaceuticals Reference Code:859133 Contact Us Email:hrop_*************

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at ******************* **Job Function:** Quality **Job Sub** **Function:** Quality Assurance **Job Category:** Professional **All Job Posting Locations:** Wilson, North Carolina, United States of America **:** The purpose of this document is to outline the job description of the QA Specialist at Janssen Biotech, Inc in Wilson, North Carolina. The employee is acquainted with the annual company and division goals and is aware of how he/she can influence these through his/her performance. **Essential Job Duties and Responsibilities** This position is responsible for ensuring compliance with regulatory requirements and company policies following current Good Manufacturing Practices, Johnson & Johnson Policies and internal procedures through the following duties and responsibilities: + Ensure the site validation program has been developed and maintained in compliance with all regulatory and corporate requirements and Master Plans. + Works with the applicable qualification teams representing Quality Assurance in the requirement, design review, construction, qualification and leveraging documentation strategies, cleaning development/validation and implementation of project. + Review and approve commissioning and qualification documentation, including URS (User Requirements Specifications), IQ (Installation Qualification), OQ (Operational Qualification), and PQ (Performance Qualification) protocols and reports, SOP's, Work Instructions and any other technical document. + Review and approves validation protocols and reports (analytical, cleaning, process, etc.) + Provide quality oversight for C&Q/CSV and validation execution activities to ensure compliance with GMP, FDA, EMA, and other regulatory requirements. + Support the development and implementation of C&Q and validation plans, ensuring alignment with project timelines and deliverables. + Perform QA reviews of system impact assessments and categorization of equipment and utilities. + Ensure compliance with company quality standards, including SOPs, work instructions, and quality policies. + Act as the QA point of contact for deviations, CAPAs, and change controls related to C&Q and validation activities. + Provide recommendations for process improvements to enhance compliance and efficiency in C&Q and validation activities. + Reviews/approves Technology Transfer documents assuring they meet regulatory and J&J requirements. + Collaborate with cross-functional teams, including engineering, validation, and manufacturing, to address quality issues. **Additional Job Duties and Responsibilities:** + Provides support and direction to all departments in respect of specific quality system elements to ensure business, quality and compliance goals are met following the J&J Standards. + Partners with other Departments to ensure that compliance systems are implemented in an efficient manner. + Develops and implements processes, procedures, forms, work instructions and tools related to the implementation of compliance systems at the site. + Carries out tasks related to the administration of site nonconformance management, change control and training systems and its applicable Electronic Tracking System (ETS). + Develops and implements processes, procedures and tools related to the implementation of compliance systems at the site. + Collaborate with cross-functional teams (Operations, Engineering & Maintenance, MSAT, QC, etc) to address quality issues. + Provides support to documentation review through evaluation and approval of documentation related to regulatory submissions, standard operating procedures (SOPs), and quality management systems to ensure accuracy and compliance as required. **Minimum Qualification** + Bachelor's degree in a scientific or engineering discipline is required. + Two to four (2-4) years of experience working within the biotherapeutic and/or pharmaceutical industry and knowledge in compliance of commissioning, qualification and validation of GMP processes and systems such as Utilities (water for injection, clean steam, process gases, HVAC, SIP/CIP), fridges, freezers, LAF, BSC units, autoclaves and isolators - as well as Process Equipment - Bioreactors, UF/DF, centrifuge, Chromatography systems. + Strong understanding of cGMP, FDA, EMA, ICH guidelines, and ISPE Baseline Guides. Hands-on experience with qualification/validation lifecycle (URS, FAT, SAT, IQ, OQ, PQ) and cleaning/process validation. + Familiarity with ISPE guidelines, including GAMP 5, ASTM E2500, and validation lifecycle principles. + Strong understanding of risk-based approaches to commissioning and qualification/validation. + Proficiency in technical writing for validation and quality documents. + Strong communication and interpersonal skills for cross-functional collaboration. **Other requirements** + An unquestionable level of integrity and commitment to operating ethically and within the boundaries of regulatory requirements. + Excellent communication and interpersonal skills, with the ability to effectively collaborate with cross-functional teams. + Proven ability to manage multiple priorities and work independently with minimal supervision. + Detail-oriented mindset, with a keen eye for identifying opportunities for process improvements. + Proven ability to prioritize tasks and meet deadlines in a dynamic manufacturing environment. + Ability to build and nurture strong and positive relationships. + The ability to work in a team environment and interact with all levels of the organization. **Required Skills:** **Preferred Skills:** Business Alignment, Business Behavior, Coaching, Compliance Management, Continuous Improvement, Data Analysis, Detail-Oriented, Goal Attainment, Human-Centered Design, Internal Controls, Issue Escalation, Problem Solving, Process Oriented, Quality Control (QC), Quality Management Systems (QMS), Quality Standards **The anticipated base pay range for this position is :** $79,000.00 - $127,650.00 Additional Description for Pay Transparency: Subject to the terms of their respective plans, employees are eligible to participate in the Company's consolidated retirement plan (pension) and savings plan (401(k)). For additional general information on Company benefits, please go to: - ********************************************* This position is eligible to participate in the Company's long-term incentive program. Subject to the terms of their respective policies and date of hire, employees are eligible for the following time off benefits: Vacation -120 hours per calendar year Sick time - 40 hours per calendar year; for employees who reside in the State of Colorado -48 hours per calendar year; for employees who reside in the State of Washington -56 hours per calendar year Holiday pay, including Floating Holidays -13 days per calendar year Work, Personal and Family Time - up to 40 hours per calendar year Parental Leave - 480 hours within one year of the birth/adoption/foster care of a child Bereavement Leave - 240 hours for an immediate family member: 40 hours for an extended family member per calendar year Caregiver Leave - 80 hours in a 52-week rolling period10 days Volunteer Leave - 32 hours per calendar year Military Spouse Time-Off - 80 hours per calendar year

We are Reckitt Home to the world's best loved and trusted hygiene, health, and nutrition brands. Our purpose defines why we exist: to protect, heal and nurture in the relentless pursuit of a cleaner, healthier world. We are a global team united by this purpose. Join us in our fight to make access to the highest quality hygiene, wellness, and nourishment a right and not a privilege. Supply Our supply chain is the backbone of our business. It's how we get our trusted products to people all over the world, safely and efficiently. And it's our talented and passionate teams that make this happen. If you're looking for a career in supply chain, there's no better place to be than Reckitt. We offer a variety of exciting opportunities in all areas of the supply chain, from planning and procurement to manufacturing and logistics. You could join our Global Supply Planning team to develop and implement our global supply strategy, or work with our Procurement Centre of Excellence team to negotiate and manage our supplier relationships. Our Manufacturing Excellence team help us improve the efficiency, quality and safety of our manufacturing operations, and our Logistics Excellence team develop new and innovative ways to distribute our products to customers. About the role The Senior Metrology Technician is responsible for ensuring the accuracy, reliability, and compliance of measurement systems and calibrated equipment within an Oral Solid Dose (OSD) pharmaceutical environment. This role focuses on calibration program management, equipment performance verification, troubleshooting, and continuous improvement of metrology practices. The Technician collaborates with production, quality, and maintenance teams to minimize downtime, maintain compliance, and support safe and efficient operations. Your responsibilities Metrology & Calibration * Perform and document calibration of instruments, temperature, pressure, humidity sensors, weigh scales, load cells, airflow devices, pH, conductivity, TOC, and measurement systems in accordance with GMP and industry standards. * Analyze calibration data to identify trends, deviations, and potential equipment reliability issues. * Lead or support root cause investigations related to measurement inaccuracies or calibration failures. * Maintain calibration standards for compliance and job readiness. * Write calibration specifications and maintain database. * Recommend technical solutions to improve measurement reliability and extend equipment lifecycle. Maintenance & Equipment Support * Support preventive and corrective maintenance activities for measurement and monitoring equipment. * Develop calibration job plans including required tools, standards, and safety requirements. * Coordinate with maintenance staff and contractors to ensure timely completion of calibration and verification tasks. * Track and report calibration KPIs such as compliance rates, overdue calibrations, and equipment performance. Documentation & Compliance * Ensure all calibration activities comply with GMP, OSHA, and company safety standards. * Partner with Quality Assurance to support audits, deviations, CAPAs, and change controls related to metrology. * Responsible for department deviations, out of tolerance reports, and all associated documentation * Maintain accurate calibration records in CMMS (e.g., SAP PM) and ensure traceability to national/international standards. Continuous Improvement * Identify opportunities to improve calibration efficiency and reduce downtime. * Train other staff and collaborate with engineers on measurement challenges and new applications. * Drive initiatives aligned with site goals such as OEE improvement and proactive calibration models. * Support capital projects and equipment upgrades with metrology expertise. This role is not currently sponsoring visas or considering international movement at this time. The experience we're looking for * Associate's degree in Metrology, Mechanical/Electrical Technology, or related technical field, or equivalent experience; bachelor's degree in engineering or related technical field preferred * 6-10+ years of experience in calibration and metrology within manufacturing environments, including pharmaceutical, chemical, food, or industrial settings * Strong knowledge of measurement principles, precision tools, calibration standards, automation, sensors, and control systems * Proficiency with CMMS systems, calibration management software, Microsoft Office, SAP, and calibration analysis tools * Experience with preventive and predictive maintenance programs * Certification in metrology or calibration technologies (e.g., ASQ CCT, CMRP) * Strong analytical and problem‑solving abilities, including root cause analysis * Effective communication and collaboration across technical and non‑technical teams * Ability to manage multiple calibration projects, prioritize tasks, and operate effectively in dynamic environments What we offer With inclusion at the heart of everything we do, working alongside our four global Employee Resource Groups, we support our people at every step of their career journey, helping them to succeed in their own individual way. We invest in the wellbeing of our people through parental benefits, an Employee Assistance Program to promote mental health, and life insurance for all employees globally. We have a range of other benefits in line with the local market. Through our global share plans we offer the opportunity to save and share in Reckitt's potential future successes. For eligible roles, we also offer short-term incentives to recognise, appreciate and reward your work for delivering outstanding results. You will be rewarded in line with Reckitt's pay for performance philosophy. Pay Range Hiring range: $37.50 - 47.00 DOE Pay Transparency The base salary range for this role will vary based on experience in job and industry, training and education, skills relevant to the position, and other factors permitted by law. In addition to the base salary, the position is eligible for an annual discretionary bonus, which is subject to change each year. Reckitt offers eligible employees competitive benefits including medical, prescription, dental, vision, and life and disability insurance; paid time off for vacation, sick and Company recognized holidays; a 401(k) plan; 16-week paid parental leave or 26 weeks for the birthing parent; adoption and fertility support; tuition reimbursement; discounts; and much more. Our compensation and benefits packages aim to give our talent the reward, protection, and peace of mind they deserve. If reasonable accommodation is needed to complete your application, please contact ******************************* .Reckitt is committed to the full inclusion of all qualified individuals. Equality We recognise that in real life, great people don't always 'tick all the boxes'. That's why we hire for potential as well as experience. Even if you don't meet every point on the job description, if this role and our company feels like a good fit for you, we still want to hear from you. All qualified applicants will receive consideration for employment without regard to age, disability or medical condition; colour, ethnicity, race, citizenship, and national origin; religion, faith; pregnancy, family status and caring responsibilities; sexual orientation; sex, gender identity, gender expression, and transgender identity; protected veteran status; size or any other basis protected by appropriate law. Nearest Major Market: Raleigh Nearest Secondary Market: Rocky Mount Job Segment: Nutrition, Counseling, Healthcare

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at ******************* **Job Function:** Technology Product & Platform Management **Job Sub** **Function:** Technical Product Management **Job Category:** People Leader **All Job Posting Locations:** Wilson, North Carolina, United States of America **Job Description:** We are searching for the best talent for an **IT - Technical Manager in Manufacturing (Technical Product Owner)** who will lead deployments and support manufacturing site technology solutions from an IT perspective. This role involves managing individual contributors and vendors, developing tactical and operational plans, to support organizational objectives and business goals. The Technical Product Owner will develop roadmaps aligning with strategic technology programs and business needs. The location for this position is **Wilson, North Carolina - USA** and requires all days 5 days on site per week. **Responsibilities** + Product owner for digital product and/or digital site services. Owns product life cycle, product roadmap and deliver of product increments. + Allocates resources to create solutions to business problems and outlines the solutions via clear and executable product requirements. Focuses and prioritizes the team's execution on the most business-critical problems. + Manages individual contributors and vendors. Develops tactical and operational plans to achieve site specific Technology Product & Platform Management goals and communicates plans to managers, supervisors, and individual contributors. + Supports financial planning and controlling. + Supports technology strategy for business partners and develops product roadmaps. + Develops insights for site leadership. Contributes to technology projects, programs, and processes. Creates reports, visualizations or other documents. Presents findings and provides updates on status to team and management. **Required qualifications** + Bachelor's degree + A minimum of 5 years' experience in a similar position + Experience in leading and managing vendors + Experience in a (pharmaceutical) manufacturing environment + Strong understanding of GMP requirements and processes + Strong experience in SDLC process + Substantial skills in manufacturing relevant IT technologies (Digital and Innovation) + Focus on Business agility and challenge thinking + Adept in ISA-95 model + Excellent written and oral communication skills, with strong interpersonal skills and a team-oriented approach. + Adept in financial management **Preferred qualifications** + Experience playing a manufacturing site level role. + Experience in pharmaceutical or life sciences industries. + Experience with manufacturing-related systems (e.g., MES PAS-X, SAP ERP, LIMS, CMMS, Truvault) and ecosystem integration. + Experience in data platforms and solutions (Azure Data Lake, GraphDB, Time Series DB) is a big plus + Experience in integrations technologies (MQTT Brokers, High Byte, Kafka,....) is a big plus + Experience in AI/ML, Model Mgmt, Data Science, Prompt Engineering, MLOps is a big plus + Familiarity with Quality-related systems (e.g Truvault, QMS,...) + Experience in solutioning and architecture. + Familiarity with OT systems and OT integrations (e.g Kepware, DeltaV, PLC,...) + Experience handling Cybersecurity + Experience in Agile, Scrum and Project Management + Understanding of product Lifecyle Johnson & Johnson is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, protected veteran status or other characteristics protected by federal, state or local law. We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act. Johnson & Johnson is committed to providing an interview process that is inclusive of our applicants' needs. If you are an individual with a disability and would like to request an accommodation, external applicants please contact us via *******************/contact-us/careers , internal employees contact AskGS to be directed to your accommodation resource. \#JNJTech **Required Skills:** Good Manufacturing Practices (GMP), Systems Development Lifecycle (SDLC) **Preferred Skills:** Agile Principles, Operational Technology (OT), Product Lifecycle

Bausch + Lomb (NYSE/TSX: BLCO) is a leading global eye health company dedicated to protecting and enhancing the gift of sight for millions of people around the world-from the moment of birth through every phase of life. Our mission is simple, yet powerful: helping you see better, to live better. Our comprehensive portfolio of over 400 products is fully integrated and built to serve our customers across the full spectrum of their eye health needs throughout their lives. Our iconic brand is built on the deep trust and loyalty of our customers established over our 170-year history. We have a significant global research, development, manufacturing and commercial footprint of approximately 13,000 employees and a presence in approximately 100 countries, extending our reach to billions of potential customers across the globe. We have long been associated with many of the most significant advances in eye health, and we believe we are well positioned to continue leading the advancement of eye health in the future. Key Activities/Responsibilities: The basic purpose of this position is to provide technical direction in the Aseptic Filling department according to the Standard Operating Procedures, to provide technical guidance through proper selection and training of staff and the work force, to insure adherence to safety, quality, and operational best practices. * Works inside the APA on an assigned line/Line type and manages the operators assigned to that line. Coaches, develops and mentors employees in areas of responsibility and supports development of employees' skills. * Reviews product batch records on the fill line for accuracy of entries, compliance to established limits and product specifications, and verifies presence of all verification signatures. * Responds to and resolves downtime issues (i.e. equipment issues and component issues). * Trains and manages employees while assuring employees understand duties, responsibilities, policies and procedures to including product batch record instructions, aseptic technique, and running of the fill line. * Troubleshoots and investigates product and process failures and documents findings in the form of process issues (PIs) and non-conformances (NCs) for assigned lines. Acts as a driver to find solutions to such issues and ensure appropriate corrective and preventive actions are taken and monitored to prevent recurrence. * Communicates to management progress of the department, problems, employee actions, new ideas, and all other pertinent information. * Interfaces with other departments and employees in a professional manner to coordinate the activities and issues that pertain to your production line (schedule adjustments, quality occurrences, etc.) Scope of Position: The Working Filling Lead is responsible for controlling the filling line including parameter setup, purging, and running production according to Standard Operating Procedures, Aseptic Technique, Bill of Materials, and Batch Records. Operates the Aseptic Filling Process and equipment to aseptically fill solution product into sterilized bottles. Monitors and inspects product during the filling process and reacts to issues by making machine and process adjustments, documenting issues, and informing the appropriate personnel of mechanical, electrical, and quality issues. Maintains the APA in orderly and aseptic condition by removing culls, documenting inspection of the work area, and performing disinfection activities as directed or required. Supports all functions of the APA as needed. Qualifications | Training: Experience: * Technical knowledge of aseptic filling equipment and all operations necessary to produce sterile products. * Excellent verbal and written communication, coaching, and teamwork skills. Ability to lead teams to achieve results. * Ability to quickly learn and effectively navigate computer-based production and quality systems. * 1-3 years aseptic manufacturing experience or advanced education degree (2 or 4 year). Preferred Skills: * Strong Reading and math comprehension * Good communication skills (written & verbal) * Good attention to detail * Demonstrated problem-solving ability * Ability to be an effective member of a team * Ability to work with minimal supervision * Ability to prioritize work and make informed decisions * Basic computer skills (i.e. MS Outlook, Excel, web-based applications) * Desire to advance leadership skills 3rd Shift | Sun-Thurs 10:30p-0700a This position may be available in the following location: Greenville, SC All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status. Job Applicants should be aware of job offer scams perpetrated through the use of the Internet and social media platforms. To learn more please read Bausch + Lomb's Job Offer Fraud Statement. Our Benefit Programs: Employee Benefits: Bausch + Lomb Applicants must be authorized to work for ANY employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time.

We are Reckitt Home to the world's best loved and trusted hygiene, health, and nutrition brands. Our purpose defines why we exist: to protect, heal and nurture in the relentless pursuit of a cleaner, healthier world. We are a global team united by this purpose. Join us in our fight to make access to the highest quality hygiene, wellness, and nourishment a right and not a privilege. Research & Development In R&D, we're full of highly skilled talents that include Scientists, Engineers, Medical, Clinical and Regulatory professionals - all working to create a cleaner, healthier world. With nine Centres of Excellence, we continually seek out new opportunities by using science, our entrepreneurial flare and our fearless innovation to develop and enhance our existing portfolio, never compromising on quality or performance. We do the right thing, always, by ensuring we act with responsibility and integrity, by complying with regulatory legislation across the globe, whilst ensuring our products are safe for our consumers and are to the highest quality. The size of our organisation means you'll have the opportunity to learn and work in different functions within R&D, giving you exposure to different disciplines, teams and environments. You will also have access to our R&D Academy, designed to develop our team and allow you to grow in our great organisation. About the role The LIMS Analyst will provide ongoing technical support to laboratories through day-to-day management of Laboratory Information Management System (LIMS) to ensure the system and managed data meet the requirements of cGMP guidelines, the global regulatory authorities for pharmaceutical development including FDA, MHRA and EMA, the relevant industry guidelines, and the Occupational Safety and Health Administration regulations. Utilize experience and knowledge to develop innovative approaches to deliver improvements in a collaborative manner across the business and influence actions through the support of others. This role is not currently sponsoring visas or considering international movement at this time. Your responsibilities * Ensure maintenance of the Laboratory Information Management System. * Maintain LIMS establishing quality standards, developing operations and troubleshooting procedures, and ensuring staff compliance. * Ensure SOP and other documents are available for LIMS processes. * Provide support for analysts in LIMS troubleshooting. * Provide general training to new analysts on LIMS operation and basic troubleshooting. * Support validation of computer software systems. * Accountable for the provision and maintenance of a safe working environment for those working in and visiting the laboratory. * Assist in all laboratory preparations for and during internal and external audits relating to LIMS and other laboratory computer systems. * May coordinate and provide response to audit actions relating to the laboratory and ensure completion of any resultant corrective and preventative actions. The experience we're looking for * BS in Science (Chemistry or related science). * 2+ years of experience in a laboratory or similar setting focusing on Laboratory Information Management System maintenance. * Analytically capable with relevant laboratory experience. * Offers accurate working practices and delivery of compliant quality documents. * Reviews and reports data relating to LIMS management. * Good understanding of pharmaceutical quality systems. * Working knowledge of IT systems. SAP, LabWare LIMS, etc. * Excellent organizational and communication skills with ability to work cross functionally. * Ideally experience of food or pharmaceutical Good Manufacturing Practice. * Ability to work on own initiative. What we offer With inclusion at the heart of everything we do, working alongside our four global Employee Resource Groups, we support our people at every step of their career journey, helping them to succeed in their own individual way. We invest in the wellbeing of our people through parental benefits, an Employee Assistance Program to promote mental health, and life insurance for all employees globally. We have a range of other benefits in line with the local market. Through our global share plans we offer the opportunity to save and share in Reckitt's potential future successes. For eligible roles, we also offer short-term incentives to recognise, appreciate and reward your work for delivering outstanding results. You will be rewarded in line with Reckitt's pay for performance philosophy. US salary ranges USD $65,000.00 - $97,000.00 Hiring Range up to 80K US pay transparency The base salary range for this role will vary based on experience in job and industry, training and education, skills relevant to the position, and other factors permitted by law. In addition to the base salary, the position is eligible for an annual discretionary bonus, which is subject to change each year. Reckitt offers eligible employees competitive benefits including medical, prescription, dental, vision, life and disability insurance; paid time off for vacation, sick, and Company recognized holidays; a 401(K) plan; generous paid parental leave; adoption and fertility support; tuition reimbursement; product discounts; and much more! If reasonable accommodation is needed to complete your application, please contact *******************************. Reckitt is committed to the full inclusion of all qualified individuals. Equality We recognise that in real life, great people don't always 'tick all the boxes'. That's why we hire for potential as well as experience. Even if you don't meet every point on the job description, if this role and our company feels like a good fit for you, we still want to hear from you. All qualified applicants will receive consideration for employment without regard to age, disability or medical condition; colour, ethnicity, race, citizenship, and national origin; religion, faith; pregnancy, family status and caring responsibilities; sexual orientation; sex, gender identity, gender expression, and transgender identity; protected veteran status; size or any other basis protected by appropriate law. Nearest Major Market: Raleigh Nearest Secondary Market: Rocky Mount Job Segment: Nutrition, Counseling, Healthcare

We are Reckitt Home to the world's best loved and trusted hygiene, health, and nutrition brands. Our purpose defines why we exist: to protect, heal and nurture in the relentless pursuit of a cleaner, healthier world. We are a global team united by this purpose. Join us in our fight to make access to the highest quality hygiene, wellness, and nourishment a right and not a privilege. About Supply Our supply chain is the backbone of our business. It's how we get our trusted products to people all over the world, safely and efficiently. And it's our talented and passionate teams that make this happen. If you're looking for a career in supply chain, there's no better place to be than Reckitt. We offer a variety of exciting opportunities in all areas of the supply chain, from planning and procurement to manufacturing and logistics. You could join our Global Supply Planning team to develop and implement our global supply strategy, or work with our Procurement Centre of Excellence team to negotiate and manage our supplier relationships. Our Manufacturing Excellence team help us improve the efficiency, quality and safety of our manufacturing operations, and our Logistics Excellence team develop new and innovative ways to distribute our products to customers. About the role Delight customers and be the backbone of our success as a Supply Intern at Reckitt. In this key role, you'll be the welcoming voice and helping hand that ensures our customers' satisfaction with every product and service. We're looking for a proactive, thoughtful individual who thrives on making a difference and improving the day of everyone they interact with. Join us to become an integral part of a team that values your expertise and is committed to excellence in service. Your responsibilities Reckitt's internships are project-based and vary depending on team and location. As an intern at our Wilson, North Carolina manufacturing facility, you will gain hands-on experience in a dynamic production environment. Responsibilities may include: * Supporting day-to-day operations on the manufacturing floor to ensure product quality and compliance with safety standards. * Assisting with process monitoring, data collection, and analysis to drive efficiency improvements. * Collaborating with cross-functional teams on projects related to packaging, quality assurance, and continuous improvement initiatives. * Learning and applying Good Manufacturing Practices (GMP) and standard operating procedures (SOPs). This role offers exposure to large-scale pharmaceutical production and an opportunity to contribute to delivering trusted healthcare products to consumers. The experience we're looking for * Students graduating with BS/BA in 2027 or 2028 * Proven background and interest in supply chain, customer service a plus, with a strong emphasis on exceptional service standards. * Highly detail-oriented with the ability to manage and prioritise a diverse workload under tight deadlines. * Comfortable working with people at all levels and eager to own responsibilities and drive improvements. * Proficient with SAP and Excel, using these tools to deliver accurate data analysis and business insights. The skills for success Supply Chain Management, Business Partnership, Collaboration, Partnership building, Relationship management, Business acumen, Productivity management, Project management, Improve business processes, Advanced analytics, Data analytics, Customer service management, Manufacturing excellence. Internship Details 10-week in-person internship program starting May 2026 Individual Projects Relocation support What we offer Salary Range $21.00 - $23.00 per hour 40 hours a week In-person Equality We recognise that in real life, great people don't always 'tick all the boxes'. That's why we hire for potential as well as experience. Even if you don't meet every point on the job description, if this role and our company feels like a good fit for you, we still want to hear from you. All qualified applicants will receive consideration for employment without regard to age, disability or medical condition; colour, ethnicity, race, citizenship, and national origin; religion, faith; pregnancy, family status and caring responsibilities; sexual orientation; sex, gender identity, gender expression, and transgender identity; protected veteran status; size or any other basis protected by appropriate law. Nearest Major Market: Raleigh Nearest Secondary Market: Rocky Mount Job Segment: Nutrition, Healthcare

Bausch + Lomb (NYSE/TSX: BLCO) is a leading global eye health company dedicated to protecting and enhancing the gift of sight for millions of people around the world-from the moment of birth through every phase of life. Our mission is simple, yet powerful: helping you see better, to live better. Our comprehensive portfolio of over 400 products is fully integrated and built to serve our customers across the full spectrum of their eye health needs throughout their lives. Our iconic brand is built on the deep trust and loyalty of our customers established over our 170-year history. We have a significant global research, development, manufacturing and commercial footprint of approximately 13,000 employees and a presence in approximately 100 countries, extending our reach to billions of potential customers across the globe. We have long been associated with many of the most significant advances in eye health, and we believe we are well positioned to continue leading the advancement of eye health in the future. Objectives | Purpose: Execute microbiological testing in support of but not limited to Environmental/Water/Bioburden monitoring, Media and lab supplies preparation, Sterility Testing and Microbial Identification. Conducts tests for in-process and finished products as well as raw materials using aseptic techniques. Compliance with all applicable procedures and practices to include local and global SOP's, product test procedures, safety, USP, ISO, GMP, and applicable governmental regulations. Key Activities/Responsibilities: Manufacturing Support through Environmental and Personnel Monitoring. Support Manufacturing operations through Environmental Monitoring. The testing consists of surface testing, employee gowning monitoring, viable air monitoring, and air total particle counts. Media and Lab Supply Preparations. Prepare culture media and supplies needed for test execution. Sterilize supplies and autoclave as required. Maintain the microbiology lab inventory. Perform Growth Promotion Testing and Sterility Verification. Water, Disinfectants, and Pre-Sterilized Product Testing. Execute testing in a Laminar Flow Hood using aseptic technique. Reading Plates and Liquid Media. Execute and document final reading of all microbiological testing. Particulate Matter Testing. Perform finished product testing in a Laminar Flow Hood and accurately document the data. Biological Indicators. Perform testing aseptically in a Laminar Flow Hood to support validation and production. Sterility Isolator Loading. Load the Sterility isolators with appropriate supplies and test samples. Execute the VHP cycle for the loaded Sterility isolators. Sterility Testing. Perform testing of finished product in an isolator. Consumables. Properly receive in ordered media and other testing supplies and document appropriately. Data Review. Review Microbiology data in a timely manner to ensure compliance to procedures, accuracy of data, and adherence to good documentation practices. Qualifications | Training: Education: BS in Biology, Microbiology or related life science Experience: Previous experience in aseptic manufacturing operations and aseptic laboratory practices highly preferred. Preferred Skills: Math to include metric conversions and ratios. Computer skills are required (Excel, Word, and other customized systems). Knowledge of basic cGMP and good documentation practices. Technical and scientific writing skills. Weekend Nights Shift: Saturday, Sunday 5:30p - 5:30a, Wednesday, Thursday 8:30p - 5:00a. This position may be available in the following location: Greenville, SC All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status. Job Applicants should be aware of job offer scams perpetrated through the use of the Internet and social media platforms. To learn more please read Bausch + Lomb's Job Offer Fraud Statement. Our Benefit Programs: Employee Benefits: Bausch + Lomb Applicants must be authorized to work for ANY employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time.

We are Reckitt Home to the world's best loved and trusted hygiene, health, and nutrition brands. Our purpose defines why we exist: to protect, heal and nurture in the relentless pursuit of a cleaner, healthier world. We are a global team united by this purpose. Join us in our fight to make access to the highest quality hygiene, wellness, and nourishment a right and not a privilege. Supply Our supply chain is the backbone of our business. It's how we get our trusted products to people all over the world, safely and efficiently. And it's our talented and passionate teams that make this happen. If you're looking for a career in supply chain, there's no better place to be than Reckitt. We offer a variety of exciting opportunities in all areas of the supply chain, from planning and procurement to manufacturing and logistics. You could join our Global Supply Planning team to develop and implement our global supply strategy, or work with our Procurement Centre of Excellence team to negotiate and manage our supplier relationships. Our Manufacturing Excellence team help us improve the efficiency, quality and safety of our manufacturing operations, and our Logistics Excellence team develop new and innovative ways to distribute our products to customers. About the role As a Senior Project Engineer specializing in tableting and coating systems, you will lead capital investment and master plan initiatives across solid dosage manufacturing operations. You'll provide technical direction and subject matter expertise in tablet compression, coating technologies, and material flow optimization. Your leadership will enhance throughput, product quality, and equipment reliability while aligning with plant performance and GMP compliance goals. Your responsibilities * Lead execution of tableting and coating scope across the project lifecycle, coordinating with cross-functional teams, consultants, and equipment suppliers to meet safety, quality, schedule, and cost targets. * Manage design phases (concept, basic, detailed) for tablet presses, coaters, and associated systems; participate in design reviews and workshops to ensure robust engineering deliverables. * Oversee procurement, installation, and qualification of tableting and coating equipment including rotary presses, perforated pan coaters, fluid bed systems, and dust control infrastructure. * Coordinate with internal stakeholders (Production, QA, Maintenance, R&D) for seamless handover of tableting and coating systems and documentation. * Support startup activities including commissioning, IQ/OQ/PQ protocols, and integration into SOPs, preventive maintenance, and QMS frameworks. * Ensure documentation adheres to GDP standards and regulatory compliance (FDA, ICH, ISO); support validation and hygiene design requirements. * Develop and manage project budgets, cash flow forecasts, and detailed implementation schedules for tableting and coating scope. * Mentor junior engineers and technicians in tablet manufacturing and coating operations. * Generate and manage engineering documentation including layout drawings, URS, material flow maps, and validation protocols. * Conduct regular project meetings to communicate progress, risks, and mitigation strategies. * Supervise contractors and installation teams to ensure workmanship meets corporate standards and supports operational integrity through startup and commissioning. The experience we're looking for * Bachelor's degree in Engineering (Mechanical, Chemical, Industrial, or related field) or equivalent experience. * 8+ years of engineering experience including 3+ years in capital project management. * Deep understanding of tablet compression, coating technologies, and solid dosage manufacturing systems. * Skilled in Microsoft Excel, Word, PowerPoint, and MS Project. * Proven experience in tableting and coating systems within pharmaceutical or OTC healthcare manufacturing environments. * Strong organizational and communication skills with ability to lead cross-functional coordination. * Proficiency in AutoCAD, equipment layout planning, and process flow mapping. * Knowledge of hygiene design, GMP logistics, and validation practices. * Understanding of project execution lifecycle and ability to drive results across diverse teams. The skills for success Supply Chain Management, Business Partnership, Collaboration and partnership building, Relationship Management, Business accumen, Productivity management, Improve business processes, Advanced Analytics, Data Analytics, Supply Chain Planning, Logistics Management. What we offer With inclusion at the heart of everything we do, working alongside our four global Employee Resource Groups, we support our people at every step of their career journey, helping them to succeed in their own individual way. We invest in the wellbeing of our people through parental benefits, an Employee Assistance Program to promote mental health, and life insurance for all employees globally. We have a range of other benefits in line with the local market. Through our global share plans we offer the opportunity to save and share in Reckitt's potential future successes. For eligible roles, we also offer short-term incentives to recognise, appreciate and reward your work for delivering outstanding results. You will be rewarded in line with Reckitt's pay for performance philosophy. Salary Range USD $115,000.00 - $173,000.00 Pay Transparency The base salary range for this role will vary based on experience in job and industry, training and education, skills relevant to the position, and other factors permitted by law. In addition to the base salary, the position is eligible for an annual discretionary bonus, which is subject to change each year. Reckitt offers eligible employees competitive benefits including medical, prescription, dental, vision, and life and disability insurance; paid time off for vacation, sick and Company recognized holidays; a 401(k) plan; 16-week paid parental leave or 26 weeks for the birthing parent; adoption and fertility support; tuition reimbursement; discounts; and much more. Our compensation and benefits packages aim to give our talent the reward, protection, and peace of mind they deserve. If reasonable accommodation is needed to complete your application, please contact *******************************. Reckitt is committed to the full inclusion of all qualified individuals. Equality We recognise that in real life, great people don't always 'tick all the boxes'. That's why we hire for potential as well as experience. Even if you don't meet every point on the job description, if this role and our company feels like a good fit for you, we still want to hear from you. All qualified applicants will receive consideration for employment without regard to age, disability or medical condition; colour, ethnicity, race, citizenship, and national origin; religion, faith; pregnancy, family status and caring responsibilities; sexual orientation; sex, gender identity, gender expression, and transgender identity; protected veteran status; size or any other basis protected by appropriate law. Nearest Major Market: Raleigh Nearest Secondary Market: Rocky Mount Job Segment: Nutrition, Counseling, Healthcare

Bausch + Lomb (NYSE/TSX: BLCO) is a leading global eye health company dedicated to protecting and enhancing the gift of sight for millions of people around the world-from the moment of birth through every phase of life. Our mission is simple, yet powerful: helping you see better, to live better. Our comprehensive portfolio of over 400 products is fully integrated and built to serve our customers across the full spectrum of their eye health needs throughout their lives. Our iconic brand is built on the deep trust and loyalty of our customers established over our 170-year history. We have a significant global research, development, manufacturing and commercial footprint of approximately 13,000 employees and a presence in approximately 100 countries, extending our reach to billions of potential customers across the globe. We have long been associated with many of the most significant advances in eye health, and we believe we are well positioned to continue leading the advancement of eye health in the future. Purpose of Job: The Principal Equipment Process Engineer will provide leadership and support of critical, value-added initiatives aligned with site priorities to implement variety of engineering projects for Lens Care Solutions manufacturing to increase machine efficiency and OEE, reduce cost, improve quality, and address critical obsolescence issues. Specify, design, and implement a portfolio of projects requiring cross-functional partnering across multiple disciplines within the organization. Position will also support day-to-day uptime needs of process equipment across the manufacturing site. Key Activities: * As technical Subject Matter Expert (SME) lead improvement projects and support daily operation of process equipment systems including packaging line equipment (cartoners, bundlers, case-packers, palletizers, printers, labellers, vision systems, robotics). Diagnose and resolve complex manufacturing technical issues and develop technical solutions to improve process performance, quality, and cost. Engage cross-disciplined resources to support implementation of improvements aligned with site priorities. Provide on-going technical support including validation, training and the creation of required documentation for new manufacturing equipment and processes. * Develop and lead Engineering projects designed to reduce waste, improve process capability, process reliability, increase OEE (Overall Equipment Effectiveness), improve quality and manage capacity as required. Develop data acquisition and performance measuring techniques to gather and analyse critical data necessary to execute actions that improve product cost, quality and manufacturing reliability. Use operational data and performance metrics to analyze critical parameters necessary to identify and drive Overall Equipment Efficiency (OEE) and reliability improvements. * Manage engineering projects including scope, resource planning, budget activities, validation and project execution timeline. Communicate status of project milestones to key stakeholders. * Advise management of new developments which may affect profit, schedule, costs, customer relations, and/or inter-departmental relations. * Maintain a working knowledge of new technologies which may improve operations and develop recommendations and plans accordingly. Identify innovative technical and process solutions that drive the desired performance in cost, quality, compliance, customer service and revenue. Qualifications Education: BS or MS degree in Mechanical, Industrial, Electrical, or Manufacturing Engineering. Advanced degree preferred. Minimum 10 years of relevant industrial experience in Pharmaceutical or Medical Device regulated manufacturing engineering with emphasis on Process & Packaging Equipment Design, process improvements, and GMP CapEx execution. Lean 6-Sigma Green Belt certification or equivalent, Certified PMP a plus Required Experience / Skills: a. Proven experience in manufacturing Process and Packaging equipment design and technology improvements in a GMP environment. b. Strong technical leadership capabilities with a proven ability to develop clear project objectives and work well in multi-disciplinary teams to solve complex problems. Proven track record of delivering to objectives. c. Solid analytical and problem-solving skills. Demonstrated proficiency in use of Process Excellence and Lean tools and Design for Six Sigma DFSS, (DMAIC, DOE, VSM, RCA, FMEA, etc.) d. Proven ability to work autonomously within a fast-paced, multitasking environment and effective at working across organizational boundaries. e. Excellent verbal and written communication skills and ability to influence at all levels of the organization. f. Strong conflict resolution, teamwork and negotiation skills, with proven ability to influence without authority. g. Proficient with the Microsoft office suite of tools including Microsoft Project, Visio, etc. h. Working knowledge of CAD software (e.g. SolidWorks) and GD&T concepts. This position may be available in the following location(s): US - Greenville, SC (Plant) All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status. Job Applicants should be aware of job offer scams perpetrated through the use of the Internet and social media platforms. To learn more please read Bausch + Lomb's Job Offer Fraud Statement. Our Benefit Programs: Employee Benefits: Bausch + Lomb Applicants must be authorized to work for ANY employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time. #LI-KF

We are Reckitt Home to the world's best loved and trusted hygiene, health, and nutrition brands. Our purpose defines why we exist: to protect, heal and nurture in the relentless pursuit of a cleaner, healthier world. We are a global team united by this purpose. Join us in our fight to make access to the highest quality hygiene, wellness, and nourishment a right and not a privilege. Supply Our supply chain is the backbone of our business. It's how we get our trusted products to people all over the world, safely and efficiently. And it's our talented and passionate teams that make this happen. If you're looking for a career in supply chain, there's no better place to be than Reckitt. We offer a variety of exciting opportunities in all areas of the supply chain, from planning and procurement to manufacturing and logistics. You could join our Global Supply Planning team to develop and implement our global supply strategy, or work with our Procurement Centre of Excellence team to negotiate and manage our supplier relationships. Our Manufacturing Excellence team help us improve the efficiency, quality and safety of our manufacturing operations, and our Logistics Excellence team develop new and innovative ways to distribute our products to customers. About the role The RPS Manager is responsible for driving a culture of continuous improvement and operational discipline across manufacturing site producing oral solid dosage and liquid products. This role leads the deployment of Lean, Six Sigma, and structured problem-solving methodologies while ensuring full compliance with cGMP, regulatory, and quality standards. This role establishes foundational performance management systems, standard ways of working, and continuous improvement capability. The position plays a critical role in supporting facility start-up, process qualification, regulatory readiness, and rapid scale-up to commercial operations. The role partners closely with Manufacturing, Quality, Engineering, Planning & Logistics, and EHS. Your responsibilities * Deploy site Operational Excellence strategy aligned with RPS and MOS; standardize processes, metrics, and ways of working across all functions. * Lead performance management systems including tiered meetings, KPI reviews, and visual management. * Drive Lean initiatives (VSM, 5S, Kaizen, standard work, waste elimination) and apply Six Sigma tools (DMAIC, SPC, RCA) to resolve complex issues and embed sustainable, cGMP‑compliant improvements. * Ensure OpEx activities meet cGMP, data integrity, and quality system requirements; partner with Quality to maintain compliance; support inspections and audits; follow change control and risk/validation processes. * Improve RFT, cycle time, throughput, OEE, asset utilization, deviations, CAPA effectiveness, inventory, and material flow; support OSD and liquid dosage manufacturing operations. * Build site OpEx capability through training, coaching, and mentoring; develop Lean leaders and Belts; drive a continuous improvement culture and mindset shift. * Use data and analytics to identify gaps and prioritize improvements; partner with IT and operations to leverage digital tools (MES, EBR, CMMS, dashboards) and enhance data accuracy and visibility. * Lead cross‑functional improvement projects; run governance forums to track initiatives, benefits, and risks; communicate progress to site and global leadership. * Quantify, validate, and sustain OpEx financial benefits (cost, productivity, capacity); support annual plans and long‑range strategy. This role is not currently sponsoring visas or considering international movement at this time. The experience we're looking for * Bachelor's degree in Engineering, Science, Pharmacy, or related field; 7-10 years in pharmaceutical or regulated manufacturing and 3-5 years in Operational Excellence, Lean, or Continuous Improvement. * Production line or facilities experience in vitamin, food, chemical, or pharmaceutical environments, with a proven track record of improving processes and systems. * Strong analytical skills and a demonstrated drive to implement improvements; Lean Six Sigma Green Belt or Black Belt. * Experience with site startup, tech transfer, or scale‑up; familiarity with MES, LIMS, SAP, and CMMS systems. * Project Management (PMP or equivalent) and/or Change Management training or certification. * Strong understanding of cGMP and pharmaceutical quality systems, with practical application of Lean, Six Sigma, and structured problem‑solving. * Knowledge of OSD and/or oral liquid manufacturing processes and experience working within change control, deviation, CAPA, and validation systems. * Ability to work effectively with incomplete data and in evolving, fast‑changing processes. The skills for success Supply Chain Management, Business Partnership, Collaboration and partnership building, Relationship Management, Business Acumen, Productivity management, Improve business processes, Advanced Analytics, Data Analytics, Supply Chain Planning, Logistics Management. What we offer With inclusion at the heart of everything we do, working alongside our four global Employee Resource Groups, we support our people at every step of their career journey, helping them to succeed in their own individual way. We invest in the wellbeing of our people through parental benefits, an Employee Assistance Program to promote mental health, and life insurance for all employees globally. We have a range of other benefits in line with the local market. Through our global share plans we offer the opportunity to save and share in Reckitt's potential future successes. For eligible roles, we also offer short-term incentives to recognise, appreciate and reward your work for delivering outstanding results. You will be rewarded in line with Reckitt's pay for performance philosophy. Salary Range USD $140,000.00 - $210,000.00 Hiring range up to 170K Pay Transparency The base salary range for this role will vary based on experience in job and industry, training and education, skills relevant to the position, and other factors permitted by law. In addition to the base salary, the position is eligible for an annual discretionary bonus, which is subject to change each year. Reckitt offers eligible employees competitive benefits including medical, prescription, dental, vision, and life and disability insurance; paid time off for vacation, sick and Company recognized holidays; a 401(k) plan; 16-week paid parental leave or 26 weeks for the birthing parent; adoption and fertility support; tuition reimbursement; discounts; and much more. Our compensation and benefits packages aim to give our talent the reward, protection, and peace of mind they deserve. If reasonable accommodation is needed to complete your application, please contact *******************************. Reckitt is committed to the full inclusion of all qualified individuals. Equality We recognise that in real life, great people don't always 'tick all the boxes'. That's why we hire for potential as well as experience. Even if you don't meet every point on the job description, if this role and our company feels like a good fit for you, we still want to hear from you. All qualified applicants will receive consideration for employment without regard to age, disability or medical condition; colour, ethnicity, race, citizenship, and national origin; religion, faith; pregnancy, family status and caring responsibilities; sexual orientation; sex, gender identity, gender expression, and transgender identity; protected veteran status; size or any other basis protected by appropriate law. Nearest Major Market: Raleigh Nearest Secondary Market: Rocky Mount Job Segment: Environmental Health & Safety, Nutrition, Pharmacy, Counseling, Healthcare

Bausch + Lomb (NYSE/TSX: BLCO) is a leading global eye health company dedicated to protecting and enhancing the gift of sight for millions of people around the world-from the moment of birth through every phase of life. Our mission is simple, yet powerful: helping you see better, to live better. Our comprehensive portfolio of over 400 products is fully integrated and built to serve our customers across the full spectrum of their eye health needs throughout their lives. Our iconic brand is built on the deep trust and loyalty of our customers established over our 170-year history. We have a significant global research, development, manufacturing and commercial footprint of approximately 13,000 employees and a presence in approximately 100 countries, extending our reach to billions of potential customers across the globe. We have long been associated with many of the most significant advances in eye health, and we believe we are well positioned to continue leading the advancement of eye health in the future. 2nd Shift - Monday - Friday 3:30pm - 12:00am The MQA Line Inspector is responsible for performing Quality inspections for finished goods & contract goods associated with products manufactured & distributed by B+L Greenville. These inspections require the use of statistical sampling plans to conduct visual and functional inspections to determine compliance with cGMP's, local / regional SOP's, and associated regulations. In addition to inspection requirements, this position will provide guidance for issue resolution, product containment, and non-conformance generation if necessary. Key Activities Utilizes statistical sampling plans to perform visual and functional inspections of contract and Greenville finished product. Documents all results in the QA batch record or on the Receiving Inspection Report. Assists in quality decisions for nonconforming product and provides QA inspection support to the Manufacturing operation. Assists in the Investigation and documentation of process issues that occur during the production operation including input to in-process product quality decisions. Maintains retain sample inventory for all finished product. Qualifications Education: High School Diploma required. Training: Pallet Jack and Fork lift. Experience: 2-3 years prior manufacturing or inspection experience required Prior exposure to visual and dimensional inspection required Previous inspection experience using balances and dimensional tools preferred. Specialized Skills: Computer skills using MS Excel, MS Word, MS Outlook, MS Access, Warehouse Management System (ERPLX) and Document Management System (Documentum). Excellent written and verbal communication skills demonstrated. Good people skills. Must be able to communicate with a cross functional team and management concerning quality issues. Decision-making ability and ability to work unsupervised expected. This position may be available in the following location: Greenville, SC All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status. Job Applicants should be aware of job offer scams perpetrated through the use of the Internet and social media platforms. To learn more please read Bausch + Lomb's Job Offer Fraud Statement. Our Benefit Programs: Employee Benefits: Bausch + Lomb Applicants must be authorized to work for ANY employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time.

We are Reckitt Home to the world's best loved and trusted hygiene, health, and nutrition brands. Our purpose defines why we exist: to protect, heal and nurture in the relentless pursuit of a cleaner, healthier world. We are a global team united by this purpose. Join us in our fight to make access to the highest quality hygiene, wellness, and nourishment a right and not a privilege. Supply Our supply chain is the backbone of our business. It's how we get our trusted products to people all over the world, safely and efficiently. And it's our talented and passionate teams that make this happen. If you're looking for a career in supply chain, there's no better place to be than Reckitt. We offer a variety of exciting opportunities in all areas of the supply chain, from planning and procurement to manufacturing and logistics. You could join our Global Supply Planning team to develop and implement our global supply strategy, or work with our Procurement Centre of Excellence team to negotiate and manage our supplier relationships. Our Manufacturing Excellence team help us improve the efficiency, quality and safety of our manufacturing operations, and our Logistics Excellence team develop new and innovative ways to distribute our products to customers. About the role The Reliability & Maintenance Engineer is responsible for developing, implementing, and optimizing maintenance and reliability strategies to ensure safe, efficient, and sustainable operation of manufacturing assets in a GMP-regulated facility. This role focuses on equipment performance analysis, preventive and predictive maintenance programs, spare parts criticality assessment, and continuous improvement initiatives. The Engineer collaborates with production, quality, and maintenance teams to minimize downtime, extend asset life, and ensure compliance with regulatory and safety standards. Your responsibilities Reliability Engineering * Analyze equipment performance data to identify trends, failure modes, and root causes. * Develop and implement reliability-centered maintenance (RCM) strategies to improve mean time between failures (MTBF) and reduce mean time to repair (MTTR). * Lead or support root cause analysis (RCA) for equipment-related deviations or failures. * Recommend engineering solutions to enhance equipment reliability and optimize lifecycle costs. Maintenance Planning & Execution * Develop, implement, and optimize preventive and predictive maintenance (PM/PdM) strategies for OSD equipment, including granulators, fluid bed dryers, tablet presses, coaters, dust collection systems, and packaging lines. * Develop detailed job plans including material lists, labor estimates, and safety requirements. * Coordinate with maintenance staff and contractors to ensure timely execution of planned work. * Track and report maintenance KPIs such as uptime, backlog, and work order completion rates. Spare Parts Criticality & Inventory Management * Conduct spare parts criticality assessments to determine which components are essential for equipment reliability and production continuity. * Classify spares into categories (critical, essential, non-critical) based on risk, lead time, and equipment impact. * Collaborate with storeroom and procurement teams to ensure availability of critical spares while optimizing inventory costs. * Evaluate repair vs. replacement decisions to balance reliability and cost-effectiveness. * Support kitting and staging of materials for planned jobs, prioritizing critical spares. * Ensure accuracy of asset hierarchies, BOMs, spare parts lists, and maintenance task plans Compliance & Safety * Ensure all maintenance and engineering activities comply with OSHA, GMP, and company safety standards. * Partner with Quality Assurance to support audits, deviations, CAPAs, and change controls. * Participate in risk assessments, LOTO procedures, and confined space protocols. Continuous Improvement * Identify opportunities to eliminate delays and improve maintenance efficiency. * Integrate predictive maintenance technologies (condition monitoring, vibration analysis, thermography). * Drive initiatives aligned with site goals such as OEE improvement and proactive maintenance models. * Support capital projects and equipment upgrades to enhance reliability. * Partner with Engineering on equipment upgrades, replacements, FAT/SAT, commissioning, and qualification. This role is not currently sponsoring visas or considering international movement at this time. The experience we're looking for * Associate's degree in a mechanical, electrical, industrial, or related technical field; bachelor's degree preferred * 3-5+ years of experience in maintenance engineering, reliability, or asset management within manufacturing, including pharmaceutical, chemical, food, or industrial environments * Strong knowledge of mechanical and electrical systems, reliability engineering principles, precision maintenance tools, PLCs, automation, and controls * Proficiency with CMMS systems, SAP, Microsoft Office, data analysis tools, and reliability analysis software * Experience with preventive and predictive maintenance programs, spare‑parts criticality analysis, and inventory optimization * Strong analytical and problem‑solving abilities, including root‑cause analysis * Effective communication and collaboration across technical and non‑technical teams * Ability to manage multiple projects, prioritize effectively, and work in dynamic environments * Knowledge of GMP documentation systems and regulatory compliance * Ability to evaluate spare‑parts criticality, balance reliability with cost efficiency, and track performance metrics to drive maintenance improvements. What we offer With inclusion at the heart of everything we do, working alongside our four global Employee Resource Groups, we support our people at every step of their career journey, helping them to succeed in their own individual way. We invest in the wellbeing of our people through parental benefits, an Employee Assistance Program to promote mental health, and life insurance for all employees globally. We have a range of other benefits in line with the local market. Through our global share plans we offer the opportunity to save and share in Reckitt's potential future successes. For eligible roles, we also offer short-term incentives to recognise, appreciate and reward your work for delivering outstanding results. You will be rewarded in line with Reckitt's pay for performance philosophy. US salary ranges USD $88,000.00 - $132,000.00 Hiring Range up to 110K US pay transparency The base salary range for this role will vary based on experience in job and industry, training and education, skills relevant to the position, and other factors permitted by law. In addition to the base salary, the position is eligible for an annual discretionary bonus, which is subject to change each year. Reckitt offers eligible employees competitive benefits including medical, prescription, dental, vision, and life and disability insurance; paid time off for vacation, sick and Company recognized holidays; a 401(k) plan; 16-week paid parental leave or 26 weeks for the birthing parent; adoption and fertility support; tuition reimbursement; discounts; and much more. Our compensation and benefits packages aim to give our talent the reward, protection, and peace of mind they deserve. If reasonable accommodation is needed to complete your application, please contact *******************************. Reckitt is committed to the full inclusion of all qualified individuals. Equality We recognise that in real life, great people don't always 'tick all the boxes'. That's why we hire for potential as well as experience. Even if you don't meet every point on the job description, if this role and our company feels like a good fit for you, we still want to hear from you. All qualified applicants will receive consideration for employment without regard to age, disability or medical condition; colour, ethnicity, race, citizenship, and national origin; religion, faith; pregnancy, family status and caring responsibilities; sexual orientation; sex, gender identity, gender expression, and transgender identity; protected veteran status; size or any other basis protected by appropriate law. Nearest Major Market: Raleigh Nearest Secondary Market: Rocky Mount Job Segment: Counseling, Nutrition, Healthcare